FDA Inspection 833308 — Genentech, Inc.

Genentech, Inc. — FEI 3006129086

The FDA completed an inspection of Genentech, Inc. on May 23, 2013 in Oceanside, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 23, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Oceanside, CA (United States)